Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A/C|Ancestral: G|Ambiguity code: V|MAF: < 0.01 (C)
Location

Chromosome 4:6301739 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM982041

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 13626, 2010_April_001_086_WFS1_606201_0005

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays